Substituent Effect on Absorption and Fluorescence Properties of Thieno[3, 2-c]Pyridine Derivatives
New substituted thieno[3,2- c ]pyridine derivatives 5 were synthesized by the reaction of 3-bromo-4-chlorothieno[3,2- c ]pyridine 1 with cyclic amine 2, which further on Suzuki reaction with boronic acids 4 converted to corresponding 3-arylthieno[3,2- c ]pyridine 5 . Substituent R 3 has predominant...
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Veröffentlicht in: | Journal of fluorescence 2017-03, Vol.27 (2), p.443-450 |
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Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | New substituted thieno[3,2-
c
]pyridine derivatives
5
were synthesized by the reaction of 3-bromo-4-chlorothieno[3,2-
c
]pyridine
1
with cyclic amine
2,
which further on Suzuki reaction with boronic acids
4
converted to corresponding 3-arylthieno[3,2-
c
]pyridine
5
. Substituent R
3
has predominant effect on fluorescence properties of thienopyridines. However, the electron donor amine at C
4
has no effect on fluorescence properties of thienopyridines.
Graphical Abstract
New thieno[3,2-c]pyridine derivatives were synthesized from 3-bromo-4-chlorothieno[3,2-c]pyridine and cyclic amines, which by on Suzuki reaction with boronic acids converted to corresponding 3-arylthieno[3,2-c]pyridine. Substituent R3 has predominant effect on fluorescence properties of thienopyridines. However, the electron donor amine at C4 has no effect on fluorescence properties of thienopyridines |
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ISSN: | 1053-0509 1573-4994 |
DOI: | 10.1007/s10895-017-2026-1 |